Novel endogenous endoplasmic reticulum transmembrane protein SURF4 suppresses cell death by negatively regulating the STING‐STAT6 axis in myeloid leukemia-Reference-Cited by-同舟云学术

Novel endogenous endoplasmic reticulum transmembrane protein SURF4 suppresses cell death by negatively regulating the STING‐STAT6 axis in myeloid leukemia

Published:2022-11-06 Issue:3 Volume:43 Page:395-399
ISSN:2523-3548
Container-title:Cancer Communications
language:en
Short-container-title:Cancer Communications

Author:

Kim Jayoung¹,Lee Hansong²,Hong Chae Mi¹,Nam Ji Ho³,Yeo Hye Ju⁴,Cho Woo Hyun⁴,Kim Hyung‐Sik⁵,Hong Changwan⁶,Kim Yun Hak²⁶^ORCID,Lee Dongjun¹^ORCID

Affiliation:

1. Department of Convergence Medicine School of Medicine Pusan National University Yangsan Gyeongsangnam‐do 50612 Republic of Korea

2. Department of Biomedical Informatics School of Medicine Pusan National University Yangsan Gyeongsangnam‐do 50612 Republic of Korea

3. Department of Radiation Oncology School of Medicine Pusan National University Yangsan Gyeongsangnam‐do 50612 Republic of Korea

4. Division of Allergy, Pulmonary, and Critical Care Medicine Department of Internal Medicine Pusan National University Yangsan Hospital Yangsan Gyeongsangnam‐do 50612 Republic of Korea

5. Department of Oral Pathology Dental and Life Science Institute School of Dentistry Pusan National University Yangsan Gyeongsangnam‐do 50612 Republic of Korea

6. Department of Anatomy School of Medicine Pusan National University Yangsan Gyeongsangnam‐do 50612 Republic of Korea

Publisher

Wiley

Subject

Cancer Research,Oncology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/cac2.12390

Reference9 articles.

1. Inhibition of Dihydroorotate Dehydrogenase Overcomes Differentiation Blockade in Acute Myeloid Leukemia

2. ER stress-induced cell death mechanisms

3. STING is an endoplasmic reticulum adaptor that facilitates innate immune signalling

4. IL-4 induces serine phosphorylation of the STAT6 transactivation domain in B lymphocytes

5. SURF4 has oncogenic potential in NIH3T3 cells

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